FDA 510(k)

DRIPRIDE PROVIDE SLIM

K-Number: K883894 · 1989-01-30

Decision Date1989-01-30

Product CodeEYQ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

DRIPRIDE PROVIDE SLIM is the device name listed in this FDA 510(k) record. The listed applicant is Weyerhaeuser Co.. It received FDA 510(k) clearance on 1989-01-30 under 510(k) number K883894. The device is classified under product code EYQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRIPRIDE PROVIDE SLIM?

DRIPRIDE PROVIDE SLIM is a medical device that received FDA 510(k) clearance on 1989-01-30. The listed applicant is Weyerhaeuser Co.. The 510(k) number is K883894.

When did DRIPRIDE PROVIDE SLIM receive FDA 510(k) clearance?

DRIPRIDE PROVIDE SLIM received FDA 510(k) clearance on 1989-01-30, under 510(k) number K883894.

Who is the listed applicant for DRIPRIDE PROVIDE SLIM?

The FDA 510(k) record lists Weyerhaeuser Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRIPRIDE PROVIDE SLIM?

The FDA product code for DRIPRIDE PROVIDE SLIM is EYQ.

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Other records listing Weyerhaeuser Co. as applicant

K883895DRIPRIDE ULTRA INCONTINENT PAD K881859DRIPRIDE DISPOSABLE UNDERPAD K872059DRIPRIDE PROVIDE ULTRA K871725DRIPRIDE DISPOSABLE UNDERPADS K854408ADULT ABSORBENT INCONTINENT BRIEF K834359ABSORBENT INCONTINENT PADS & BRIEFS

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Related Devices (Code: EYQ)

K950784DRISTAR URINARY INCONTINENCE MANAGEMENT SYSTEMAdvanced Bioresearch Assoc.K932310KIT PAK INCONTINENT SKIN CARE KITKit Pak, Inc.K903342DEODORIZING AND SOUND MUFFLING ANAL PADBiological Resistance, Inc.K891686LIB SYSTEM, BABY/ADULT DIAPERIntera Corp.K885185INTERA SHIELD AND INTERA UNDERGARMENTIntera Corp.K883895DRIPRIDE ULTRA INCONTINENT PADWeyerhaeuser Co.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.